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Study identifier: NCT06896916 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study of Intravenously (IV) Infused Etentamig in Combination With an Oral Cereblon E3 Ligase Modulatory Drug (CELMoD) Agent Assessing Adverse Events and Change in Disease Activity in Adult Participants With Relapsed or Refractory Multiple Myeloma

Condition: Multiple Myeloma  ·  Sponsor: AbbVie

PhasePhase 1
Planned participants135
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Multiple myeloma (MM) is a plasma cell disease characterized by the growth of clonal plasma cells in the bone marrow. The purpose of this study is to assess the adverse events and change in disease activity of etentamig in combination with a cereblon E3 ligase modulatory drug (CELMoD) agent in adult participants with relapsed/refractory (R/R) multiple myeloma (MM). Adverse events and change in disease state will be assessed. Etentamig is an investigational drug being developed for the treatment of R/R MM. Study doctors put the participants in groups called treatment arms. Multiple doses of etentamig in combination with iberdomide will be explored. Each treatment arm receives a different dose of etentamig and iberdomide to determine a tolerable dose. Approximately 135 adult participants with R/R MM will be enrolled in the study in approximately 50 sites worldwide. In phase 1 participants will receive escalating intravenous (IV) etentamig in combination with oral iberdomide. In phase 2 participants will receive IV etentamig at one of two doses in combination with oral iberdomide, as part of the approximately 129 month study duration. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at an approved institution (hospital or clinic). The effect of the treatment will be frequently checked by medical assessments, blood tests, questionnaires and and monitoring of side eff…

This description comes directly from the study's public registry record.

Talk to the study team

ABBVIE CALL CENTER  ·  844-663-3742  ·  abbvieclinicaltrials@abbvie.com

Always discuss trial participation with your own doctor first.

Locations (27)

Beverly Hills Cancer Center /ID# 266921Beverly Hills, California, United StatesRecruiting
Colorado Blood Cancer Institute /ID# 273751Denver, Colorado, United StatesRecruiting
Washington University /ID# 266972St Louis, Missouri, United StatesRecruiting
Rutgers Cancer Institute of New Jersey /ID# 266833New Brunswick, New Jersey, United StatesRecruiting
Memorial Sloan Kettering Cancer Center - New York - York Avenue /ID# 270282New York, New York, United StatesRecruiting
University Of North Carolina Health Care - Hillsborough Campus /ID# 278230Hillsborough, North Carolina, United StatesRecruiting
Swedish Medical Center - Seattle /ID# 268052Seattle, Washington, United StatesRecruiting
Blacktown Hospital /ID# 265983Blacktown, New South Wales, AustraliaRecruiting
Wollongong Hospital /ID# 265625Wollongong, New South Wales, AustraliaRecruiting
The Alfred Hospital /ID# 265981Melbourne, Victoria, AustraliaRecruiting
Austin Hospital /ID# 265984Melbourne, Victoria, AustraliaRecruiting
Sir Charles Gairdner Hospital /ID# 265985Nedlands, Western Australia, AustraliaRecruiting

+ 15 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06896916